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Pharma training for United States: 271 courses on selling and complying abroad

Pharma companies from United States face the same questions when they sell abroad: which regulator decides, which guideline the auditor reads, how the buyer on the other side of the table thinks, and what the objections sound like in that market. Pharma Lectures has 271 audio courses written for teams from United States, covering regulatory affairs, good manufacturing and distribution practice, business development and export sales, and the culture of each target market. One licence covers every employee of the legal entity for twelve months, in three lengths per module, with workbook, transcript, sourced facts, a certificate per learner and a recorded training record. Prices start at €1,950 and a free sample module can be requested for any course.

The 271 courses, with the price for your company size

Prices are for the whole company, 12 months. Pick your company size once; the site remembers it.

How a Pharma Lectures course works

Every title is one licence for the whole legal entity, twelve months, every employee. Each module exists in three lengths: 10, 25 or 50 minutes, by role. Each module ends with a recorded multiple-choice questionnaire, so the training record is complete for the auditor. Delivered within 72 hours of payment.

  • Audio modules in all three lengths, included in every purchase. The briefing for the board and the sales floor, the standard run for regulatory and quality, the expanded walk-through for the bench. One price buys all three; each person takes the length their role needs. Listen on the commute, at the bench, in the car.
  • Made to be listened to. A narrator with character, a story in every module and real examples from the buyer's side of the table. Not a read-out of the guideline that puts the room to sleep.
  • Companion workbook. Exercises and checklists per module, ready to file.
  • Full transcript. Searchable, printable, quotable in your procedures.
  • Source for every fact. Each statement links to its guideline, regulation or paper, so an auditor can check it.
  • Certificate per learner. Name, course, hours, guideline version, date.
  • Auditable training record. Per-person export for your quality file, the document inspectors ask for under EU GMP Chapter 2.

Free sample module

Hear one full module before you spend a cent. Send your company and the role you want trained, and a complete sample module comes back with its workbook and transcript.

Request the free sample on WhatsApp

or email [email protected], or leave your details: